Evaluation of the acceptability of patient-reported outcome measures in women following pelvic floor procedures

被引:5
|
作者
Ruseckaite, Rasa [1 ]
Bavor, Claire [1 ]
Marsh, Lucy [1 ]
Dean, Joanne [1 ]
Daly, Oliver [1 ,2 ]
Vasiliadis, Dora [3 ]
Ahern, Susannah [1 ]
机构
[1] Monash Univ, Dept Epidmiol & Prevent Med, Melbourne, Vic 3004, Australia
[2] Western Hlth, Dept Obstet & Gynaecol, Melbourne, Vic, Australia
[3] Australian Pelv Floor Procedure Registry, Consumer Representat, Melbourne, Vic, Australia
关键词
Stress urinary incontinence; Registry; Acceptability; Quality of life; QUALITY-OF-LIFE; INCONTINENCE SEXUAL QUESTIONNAIRE; URINARY-INCONTINENCE; DISORDERS REGISTRY; GLOBAL IMPRESSION; VALIDATION; SYMPTOMS; DESIGN; ICIQ;
D O I
10.1007/s11136-022-03099-x
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Purpose Patient-reported outcome measures (PROMs) are valuable tools in evaluating the outcomes of surgical treatment health-related quality of life (HRQoL) of women with stress urinary incontinence (SUI) and may be incorporated into related clinical quality registries. The aim of this study was to assess the feasibility and acceptability of incorporating PROMs into the Australian Pelvic Floor Procedure Registry (APFPR). Methods Semi-structured qualitative interviews were conducted with women with SUI (N = 12) and their managing clinicians (N = 11) in Victoria, Australia. Interview topics covered content and face validity, appropriateness, and acceptability of three incontinence-specific, two pain, one anxiety and depression, one sexual function and one patient global impression of improvement instruments identified through the literature to determine their suitability and acceptability for the APFPR. We analysed interview data into topics using conventional content analysis. Results Study participants agreed that PROMs were needed for the APFPR. Both participant groups suggested that some of the instruments were ambiguous, therefore only three instruments (one incontinence-specific, sexual function and patient global impression of improvement) will be included in the APFPR. Both clinicians and women agreed it would be appropriate to answer PROMs at baseline and then at 6- and 12-month postsurgically. Email, phone call and mail-out of the instruments were the preferred options for administration. Conclusion Most women and clinicians supported the feasibility of incorporating PROMs in the APFPR. Participants believed the PROMs would demonstrate useful aggregate HRQoL data and have potential for use in individual care.
引用
收藏
页码:2213 / 2221
页数:9
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